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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508995Generated: November 2, 2026

Phosphorus trichloride → 4-chloro-2-isopropoxy-6,7-dihydro-5H-cyclopenta[b]pyridine

https://huagongshe.com/reaction/1508995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
Reactant4-chloro-2-isopropoxy-6,7-dihydro-5H-cyclopenta[b]pyridine oxideHCID 90110772—
SolventDichloromethaneHCID 6344—
Product4-chloro-2-isopropoxy-6,7-dihydro-5H-cyclopenta[b]pyridineHCID 9011237377%

Reaction Steps

To a solution of 4-chloro-2-isopropoxy-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide (0.079 g, 0.35 mmol) in methylene chloride (5 mL) was added phosphorous trichloride (0.096 g, 0.70 mmol). The mixture stirred at rt for 30 min. After this time, the mixture was quenched with a saturated solution of NaHCO3 and extracted with methylene chloride. The organic layer were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound (0.057 g, 77%) as a clear oil. MW=211.69. 1H NMR (CDCl3, 300 MHz) δ 6.47 (s, 1H), 5.27-5.18 (m, 1H), 3.01-2.84 (m, 4H), 2.11 (quin, J=7.5 Hz, 2H), 1.31 (d, J=6.0 Hz, 6H); APCI MS m/z 212 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-79be5676ea8d42ba819c1d2d3af0385b
Source noteuspto-grants-2015_12